Ethyl ( E )-4-( 2 , 4-Dimethoxyphenyl )-6-( 2 , 4-dimethoxystyryl )-2-oxo-1 , 2 , 3 , 4-tetrahydropyrimidine-5-carboxylate

A new compound belonging to the “heterostilbene” derivative, namely ethyl (E)-4-(2,4dimethoxyphenyl)-6-(2,4-dimethoxystyryl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate (2), has been successfully synthesized as an unprecedented side product of the Biginelli reaction between 2,4-dimethoxybenzaldehyde, ethyl acetoacetate and urea, employing PTSA as catalyst in reflux conditions and using ethanol as solvent. The molecular structure of compound (2) was established by FTIR, HRESIMS, 1D and 2D NMR.

In this paper, we report a compound which differs from the product generated from both of the Biginelli-type reactions mentioned above.Despite the similarity of its reaction pattern to the Biginelli-type reaction producing arylidenepyrimidinone, there is a difference in the carbonyl component used.The aforementioned Biginelli-type reaction uses a cyclic mono carbonyl component that has two kinds of acidic C-H with equivalent reactivity, such as cyclopentanone [5][6][7][8][9][10], cyclohexanone [9][10][11] and cyclooctanone [9], so that it yields a bicyclic arylidenepyrimidinone.Interestingly, in our experiment, we used an acyclic 1,3-dicarbonyl component that possessed two acidic C-H moieties with different reactivities, namely ethyl acetoacetate.Consequently, we obtained a DHPM derivative attaching styryl moiety at C-6 (2).

Results and Discussion
Compound 2 was isolated as a side product from the Biginelli reaction between 2,4-dimethoxybenzaldehyde, ethyl acetoacetate and urea using PTSA as catalyst in reflux condition in ethanol (Figure 1).Separation of compound 2 from the main product, namely ethyl 4-(2,4dimethoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate (1), was conducted by column chromatography.Under our reaction conditions, we obtained more product 2 than product 1, although compound 2 is a side product.We got 152 mg (15.6%) of compound 1 and 402 mg (28.6%) of compound 2. Both compounds were successfully separated, their purity analyzed by TLC, and their structure then determined using spectroscopic evidence.In this paper, we do not discuss compound 1, because it has been reported previously [12].product 1, although compound 2 is a side product.We got 152 mg (15.6%) of compound 1 and 402 mg (28.6%) of compound 2. Both compounds were successfully separated, their purity analyzed by TLC, and their structure then determined using spectroscopic evidence.In this paper, we do not discuss compound 1, because it has been reported previously [12].The usage of the catalyst PTSA for the Biginelli reaction has often been reported.This catalyst can be used under various reaction conditions, such as reflux in ethanol [13], grindstone [14], microwave [15] and ultrasonic irradiation [16].However, these reaction conditions give only the main product, and do not provide side products such as compound 2. Seemingly, the amount of catalyst used has an effect on the formation of side products.The reaction condition mentioned used PTSA in a relatively low amount (<15%).In contrast with our experiment based on ethyl acetoacetate, we used 33 mol% of the catalyst.The reaction between compound 1 and 2,4-dimethoxybenzaldehyde using 33% PTSA as catalyst gave no product.This observation led to the argument that compound 2 was formed through a one-step multicomponent reaction, competing with the formation reaction of compound 1.Therefore, we propose a reaction pathway which starts with an aldol condensation between ethyl acetoacetate and 2,4-dimethoxybenzaldehyde to produce intermediate 5, which is a γ,δ-unsaturated dicarbonyl compound.A subsequent Biginelli reaction then generates compound 2 (see Figure 2).The usage of the catalyst PTSA for the Biginelli reaction has often been reported.This catalyst can be used under various reaction conditions, such as reflux in ethanol [13], grindstone [14], microwave [15] and ultrasonic irradiation [16].However, these reaction conditions give only the main product, and do not provide side products such as compound 2. Seemingly, the amount of catalyst used has an effect on the formation of side products.The reaction condition mentioned used PTSA in a relatively low amount (<15%).In contrast with our experiment based on ethyl acetoacetate, we used 33 mol% of the catalyst.The reaction between compound 1 and 2,4-dimethoxybenzaldehyde using 33% PTSA as catalyst gave no product.This observation led to the argument that compound 2 was formed through a one-step multicomponent reaction, competing with the formation reaction of compound 1.Therefore, we propose a reaction pathway which starts with an aldol condensation between ethyl acetoacetate and 2,4-dimethoxybenzaldehyde to produce intermediate 5, which is a γ,δ-unsaturated dicarbonyl compound.A subsequent Biginelli reaction then generates compound 2 (see Figure 2).product 1, although compound 2 is a side product.We got 152 mg (15.6%) of compound 1 and 402 mg (28.6%) of compound 2. Both compounds were successfully separated, their purity analyzed by TLC, and their structure then determined using spectroscopic evidence.In this paper, we do not discuss compound 1, because it has been reported previously [12].The usage of the catalyst PTSA for the Biginelli reaction has often been reported.This catalyst can be used under various reaction conditions, such as reflux in ethanol [13], grindstone [14], microwave [15] and ultrasonic irradiation [16].However, these reaction conditions give only the main product, and do not provide side products such as compound 2. Seemingly, the amount of catalyst used has an effect on the formation of side products.The reaction condition mentioned used PTSA in a relatively low amount (<15%).In contrast with our experiment based on ethyl acetoacetate, we used 33 mol% of the catalyst.The reaction between compound 1 and 2,4-dimethoxybenzaldehyde using 33% PTSA as catalyst gave no product.This observation led to the argument that compound 2 was formed through a one-step multicomponent reaction, competing with the formation reaction of compound 1.Therefore, we propose a reaction pathway which starts with an aldol condensation between ethyl acetoacetate and 2,4-dimethoxybenzaldehyde to produce intermediate 5, which is a γ,δ-unsaturated dicarbonyl compound.A subsequent Biginelli reaction then generates compound 2 (see Figure 2).This reaction pathway differs from the pathway suggested by Zhang et al. (2015), who proposed that product 1 is an intermediate in the reaction that was conducted using the Lewis acid catalyst, FeCl 3 •6H 2 O [17].Besides the different catalyst, the 1,3-dicarbonyl component used by Zhang was an acetoacetanilide derivative.However, our proposed reaction pathway requires further proof, because we did not verify the existence of intermediate 5 during the reaction process.In addition, the nucleophilicity of ethyl acetoacetate at the γ position is relatively low, except under strongly basic conditions, where a dianion can be formed [18,19].S1).From the IR spectrum following groups N-H, the amide bond types C-H aliphatic, C=O amide type, conjugated C=C, and C-O-C alkyl-aryl ether were identified, respectively, and are exhibited by absorption band at v max (cm −1 ) 3266, 2927, 1685, 1607, 1503 and 1270 (see Supplementary Material, Figure S2).Analysis of 1 H-NMR (Table 1) indicating two aromatic protons with orto coupling [δ H 7.59 (d, J = 8.6 Hz) and 7.01 (d, J = 8.4 Hz], two aromatic protons showing orto and meta coupling [δ H 6.51 (dd, J = 8.6, 2.3 Hz) dan 6.36 (dd, J = 8.4, 2.2 Hz)], and two aromatic protons showing meta coupling [δ H 6.46 (d, J = 2.2 Hz) and 6.44 (d, J = 2.3 Hz)].This evidence indicated two aromatic rings, each possessing three protons with ABX systems.The signal of two olefinic protons, shown as two doublet signals at 8.09 and 7.30 ppm with J = 17.0 Hz, indicated the existence of an E geometric alkene.The signal at 5.73 ppm showed a benzylic or allylic proton closed to electronegative atom (nitrogen).The presence of four methoxy groups is shown by four singlet signals with an integration value of 12 at δ H 3.85-3.77ppm.The presence of multiplet signal at 4.09 ppm with an integration value of 2 and a triplet signal at 1.14 ppm with an integration value of 3 showed the existence of an ethoxy moiety possessing diastereotopic protons at CH 2 moiety (see Supplementary Materials, Figures S3  and S4).In 13 C-NMR (Table 1), the 25 signals shown represent all carbon atoms of compound 2 (see Supplementary Materials, Figure S5).Based on the results of the HMQC experiment, we observed two protons forming no correlation with carbon atoms, namely singlet proton signal at δ H at 6.83 and 5.67 ppm.This indicated that both protons were attached to a heteroatom, namely nitrogen.Furthermore, it was observed that a proton at δ H 5.73 ppm attached to a carbon atom at δ H 50.0 ppm (see Supplementary Materials, Figure S6).This showed that the proton is a benzylic-allylic attached to nitrogen, which is characteristic for 3,4-dihydropyrimidinone with aryl substituent at C-4.In addition, the existence of the 3,4-dihydropyrimidinone scaffold was also supported by the results of the HMBC experiment, which showed a correlation between the proton at C-4 with conjugated olefinic carbon (δ C 99 ppm (C-5) and 145.2 ppm (C-6) the and urea carbonyl type (δ C 153.1, C-2).The presence of the aryl group at C-4 is proved by a long-range correlation of the C-4 proton with three aromatic protons [δ C 122.4 (C-15), 157.9 (C-16), and 127.5 (C-20)].Long-range correlation of the C-4 proton with the carbon atom δ C 165.8 ppm indicated that the conjugated carbonyl ester was attached to C-5.The position of styryl moiety at C-6 is proved by the long-range correlation of proton H-1 (δ H 6.83 ppm) with olefinic carbon (δ C 117.4.C-7).In addition, both olefinic protons [7.30 (H-7) and 8.09 (H-8)] built long-range correlations with C-6.The long-range correlations of the HMBC experiment that are possible with the structure of compound 2 are displayed in Figure 3 and in Figure S7 in the Supplementary Materials.Based on the structure elucidation, it can be concluded that compound 2 is a new compound, and it has not been previously identified in the literature.Based on the results of the HMQC experiment, we observed two protons forming no correlation with carbon atoms, namely singlet proton signal at δH at 6.83 and 5.67 ppm.This indicated that both protons were attached to a heteroatom, namely nitrogen.Furthermore, it was observed that a proton at δH 5.73 ppm attached to a carbon atom at δH 50.0 ppm (see Supplementary Materials, Figure S6).This showed that the proton is a benzylic-allylic attached to nitrogen, which is characteristic for 3,4dihydropyrimidinone with aryl substituent at C-4.In addition, the existence of the 3,4-

Figure 3
Figure 3 (a) Numbering of the structure, and (b) Selected HMBC correlations for compound 2.

Figure 3 .
Figure 3. (a) Numbering of the structure, and (b) Selected HMBC correlations for compound 2.

Table 1 .
NMR data of compound 2 in CDCl 3 .